83191-44-0

Upstream product

• 83703-39-3 ((E)-1-Methyl-but-2-enyl)-p-tolyl-amine 
• 106-49-0 p-toluidine 
• 83703-39-3 ((E)-1-Methyl-but-2-enyl)-p-tolyl-amine 

Downstream Products

• 1411933-72-6 4-methyl-N-{4-methyl-2-[(2E)-1-methylbut-2-en-1-yl]phenyl}benzenesulfonamide 
• 1411933-76-0 N-{4-methyl-2-[(2E)-1-methylbut-2-en-1-yl]-phenyl}-2-nitrobenzenesulfonamide 
• 73177-34-1 2-ethyl-3,5-dimethyl-1H-indole 

Relevant academic research and scientific papers

Synthesis of (1′S*,2R*,3R*)- and (1′S*,2R*,3S*)-N-arylsulfonyl-2-(1′-halogenethyl)-3-methylindolines and their selective toxicity against SH-SY5Y cell line

N-tosyl-2- and N-tosyl-4-halogen-substituted derivatives of 2-(1-methylbut-2-en-1-yl)aniline were synthesized and their molecular iodine-mediated cyclization was investigated. The cyclization upon interaction of N-tosyl-6-methyl-2-(1-methylbut-2-en-1-yl)a

Approach to preparative synthesis of ortho-(1-methylbut-2-en-1-yl)anilines, precursors of new cytotoxic heterocycles

The reaction of aromatic Claisen rearrangement of N-(1-methylbut-2-en-1-yl)anilines in the presence of p-toluenesulfonic acid was investigated. N-Tosyl-2-(1-iodoethyl)-3-methylindoline derivatives were obtained; one of them exhibited a cytotoxic activity.